Zhong Shan, Wang Li, Mei Xue-Ling
Department of Dermatology, Beijing Friendship Hospital, Capital Medical University, Beijing, China.
J Int Med Res. 2019 Aug;47(8):3918-3925. doi: 10.1177/0300060519859739. Epub 2019 Jul 15.
Desmoplastic trichilemmoma (DT) of the scalp is a rare disease. In this report, we describe a 67-year-old man who had a small papule lesion around the hairline of the left scalp for more than 40 years. The lesion had rapidly grown to become a solitary, round, 15-mm neoplasm within 6 months. Histopathological examination showed that the mass was composed of a peripheral layer of columnar cells with nuclear palisading resembling the outer root sheath; the mass was surrounded by a thickened glassy basement membrane. The stroma in the center of the mass displayed solid, hyaline degeneration and an eosinophilic pattern, streaked with epithelial cords or islands. Immunohistochemical evaluation showed diastase-resistant, periodic acid–Schiff-positive desmoplastic stroma at the center, and Ber-EP4-negative tumor cells (CD34-positive focally and Bcl-2-positive at the periphery). The tumor was completely resected, and no recurrence occurred during the follow-up period. In this report, we also summarize immunohistochemical features from previous reports of DT, facilitating differential diagnosis of DT from some invasive skin tumors.
头皮促纤维增生性毛根鞘瘤(DT)是一种罕见疾病。在本报告中,我们描述了一名67岁男性,其在左头皮发际线周围出现一个小丘疹病变已40多年。该病变在6个月内迅速生长为一个孤立的、圆形的、15毫米的肿瘤。组织病理学检查显示,肿块由一层外周柱状细胞组成,细胞核呈栅栏状排列,类似外根鞘;肿块被增厚的玻璃样基底膜包围。肿块中心的间质呈现实性、透明变性和嗜酸性模式,有上皮条索或岛状条纹。免疫组化评估显示,中心为抗淀粉酶、过碘酸-希夫染色阳性的促纤维增生性间质,肿瘤细胞Ber-EP4阴性(局部CD34阳性,外周Bcl-2阳性)。肿瘤被完全切除,随访期间未复发。在本报告中,我们还总结了既往DT报告中的免疫组化特征,有助于DT与一些侵袭性皮肤肿瘤的鉴别诊断。